GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dgoD in Caulobacter crescentus NA1000

Align galactonate dehydratase (EC 4.2.1.6) (characterized)
to candidate CCNA_00566 CCNA_00566 mannonate dehydratase

Query= BRENDA::G3Y8T6
         (383 letters)



>FitnessBrowser__Caulo:CCNA_00566
          Length = 403

 Score =  184 bits (466), Expect = 5e-51
 Identities = 123/374 (32%), Positives = 186/374 (49%), Gaps = 44/374 (11%)

Query: 19  VKVTDSEDKFGWGEATLEGHTQAVEGAL-DEIIGRIVGYEADDIEHVWQTIWRLGFYRGG 77
           +K+T  +   G G+ATL G   +V   L D ++  ++G +A  IE +WQ  +R  ++RGG
Sbjct: 21  LKITTEDGITGVGDATLNGRELSVVSFLQDHMVPSLIGRDAHQIEDIWQFFYRGSYWRGG 80

Query: 78  PVFMSALSGIDIALWDLKGRRLNVPVYQLLGGKVRNKVQVYAWIGGDRPSDVEVAAKARI 137
           PV M+AL+ +D+ALWD+KG+   +PVYQLLGG  R  V VY    G+   D    A    
Sbjct: 81  PVAMTALAAVDMALWDIKGKVAGLPVYQLLGGACRTGVTVYGHANGETIEDTIAEAVKYK 140

Query: 138 AQGLKCVKMN---------------------ATEDM---NWLDSPSVLDSC---IERIKQ 170
           A G K +++                      A  D+   N   +   L+S     ER ++
Sbjct: 141 AMGYKAIRLQTGVPGLASTYGVSKDKMFYEPADNDLPTENIWSTAKYLNSVPKLFERARE 200

Query: 171 VKALGLDAGL--DFHGRLHRPMAKQLAKALEPYRPLFIEEPLLVEHPEAIKQLSQHTTIP 228
           V  LG D  L  D H RL    A +L K LEPYR  ++E+ +  E+    + + QHTT P
Sbjct: 201 V--LGWDVHLLHDVHHRLTPIEAARLGKDLEPYRLFWLEDSVPAENQAGFRLIRQHTTTP 258

Query: 229 IAFGERLYTRWDVKRFLEDASVDVLQPDIAHAGGISETKRIATMAETYDVAIAPH--CPL 286
           +A GE     WD K+ +E+  +D L+  + HAGGI+  K+IA  A+ + V    H    L
Sbjct: 259 LAVGEIFAHVWDAKQLIEEQLIDYLRATVLHAGGITNLKKIAAFADLHHVKTGCHGATDL 318

Query: 287 GPIALAASMQVALSTPNFVIQEMSLGMHYNVEAGDIDLTSYLTNPTVFNIEEGYVPAPTG 346
            P+ +AA++   +S  NF +QE    M +  E   +        P  +   +G +     
Sbjct: 319 SPVTMAAALHFDMSITNFGLQEY---MRHTPETDAV-------FPHAYTFSDGMLHPGDK 368

Query: 347 AGLGVEIDEELVRR 360
            GLGV+IDE+L  +
Sbjct: 369 PGLGVDIDEDLAAK 382


Lambda     K      H
   0.320    0.138    0.425 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 440
Number of extensions: 30
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 383
Length of database: 403
Length adjustment: 31
Effective length of query: 352
Effective length of database: 372
Effective search space:   130944
Effective search space used:   130944
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory